Hugh Gurling
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(Suggest an Edit or Addition)According to Wikipedia, Hugh Malcolm Douglas Gurling was an English medical geneticist who specialised in the role of genetics and mental health. He led a molecular psychiatry laboratory at University College, London. Gurling was born in London on 6 May 1950, and brought up in Derbyshire. His father, Kenneth Gurling, was a physician and inaugural dean of the University of Nottingham. His mother, Nonie Sempill, was a nurse.
Hugh Gurling's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) (6445)
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
- Common variants in ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer’s disease (2011) (1701)
- Genome-wide association study identifies five new schizophrenia loci (2011) (1680)
- Letter abstract - Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's Disease (2009) (1644)
- Rare chromosomal deletions and duplications increase risk of schizophrenia (2008) (1506)
- Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease, and shows evidence for additional susceptibility genes (2009) (1441)
- Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (2013) (1388)
- Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. (2003) (1195)
- Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder (2008) (1189)
- A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) (1125)
- Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (2011) (929)
- The UK10K project identifies rare variants in health and disease (2015) (926)
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) (736)
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
- Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. (2003) (592)
- Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease (2010) (587)
- Localization of a susceptibility locus for schizophrenia on chromosome 5 (1988) (572)
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
- Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23. (2001) (396)
- Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) (296)
- Molecular genetic evidence for heterogeneity in manic depression (1987) (261)
- An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation (2016) (249)
- Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
- Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8. (1996) (175)
- Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23‐q24, and suggests the presence of additional loci on 1p and 1q (2003) (163)
- A microarray gene expression study of the molecular pharmacology of lithium carbonate on mouse brain mRNA to understand the neurobiology of mood stabilization and treatment of bipolar affective disorder (2007) (151)
- A comprehensive family-based replication study of schizophrenia genes. (2013) (144)
- A genomewide association study of response to lithium for prevention of recurrence in bipolar disorder. (2009) (142)
- A genome-wide association study of attempted suicide (2011) (140)
- Genome-wide association study of suicide attempts in mood disorder patients. (2010) (132)
- Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport (2016) (131)
- Mutation screening of X‐chromosomal neuroligin genes: No mutations in 196 autism probands (2004) (129)
- Genetics of attention-deficit hyperactivity disorder (ADHD) (2009) (127)
- Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual. (2000) (119)
- Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1 (2014) (115)
- Genome-wide Association Study of Alzheimer’s disease with Psychotic Symptoms (2011) (114)
- Genetic correlation between amyotrophic lateral sclerosis and schizophrenia (2017) (107)
- Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia. (2006) (98)
- Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness. (2011) (94)
- Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22. (1997) (93)
- Lack of normal pattern of cerebral asymmetry in familial schizophrenic patients and their relatives — The Maudsley Family Study (1999) (92)
- Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
- Brain changes in schizophrenia (1998) (91)
- Genetic association analysis of serotonin system genes in bipolar affective disorder. (1999) (89)
- Exclusion of linkage to 5qll13 in families with schizophrenia and other psychiatric disorders (1989) (89)
- NK1 (TACR1) Receptor Gene ‘Knockout’ Mouse Phenotype Predicts Genetic Association with ADHD (2010) (87)
- An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locus. (2000) (85)
- A rare functional noncoding variant at the GWAS-implicated MIR137/MIR2682 locus might confer risk to schizophrenia and bipolar disorder. (2014) (84)
- Case–case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes (2011) (83)
- Linkage findings in bipolar disorder (1995) (83)
- Computerized tomography and neuropsychological assessment in long-term high-dose heroin addicts. (1989) (81)
- Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14 (2006) (77)
- Autosomal Dominant Gene Transmission in a Large Kindred with Gilles de la Tourette Syndrome (1992) (76)
- The Epsin 4 gene on chromosome 5q, which encodes the clathrin-associated protein enthoprotin, is involved in the genetic susceptibility to schizophrenia. (2005) (74)
- Cloning of the human dopamine D5 receptor gene and identification of a highly polymorphic microsatellite for the DRD5 locus that shows tight linkage to the chromosome 4p reference marker RAF1P1. (1993) (73)
- Enhanced cationic liposome-mediated transfection using the DNA-binding peptide μ (mu) from the adenovirus core (2001) (69)
- A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans (2014) (69)
- Twin and adoption studies. How good is the evidence for a genetic role? (1983) (68)
- Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (2009) (64)
- Depression, criminality and psychopathology associated with alcoholism: evidence from a twin study. (1984) (62)
- The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. (2012) (61)
- A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts (2020) (60)
- New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. (2015) (58)
- Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder (2011) (58)
- Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome (2006) (57)
- Support of association between BRD1 and both schizophrenia and bipolar affective disorder (2010) (55)
- No Evidence for a Susceptibility Locus Predisposing to Manic Depression in the Region of the Dopamine (D2) Receptor Gene (1991) (55)
- Evidence for the association of the DAOA (G72) gene with schizophrenia and bipolar disorder but not for the association of the DAO gene with schizophrenia (2009) (52)
- The genetic susceptibility to Gilles de la Tourette Syndrome in a large multiple affected british kindred: Linkage analysis excludes a role for the genes coding for dopamine D1, D2, D3, D4, D5 receptors, dopamine beta hydroxylase, tyrosinase, and tyrosine hydroxylase (1995) (49)
- Analysis of ANK3 and CACNA1C variants identified in bipolar disorder whole genome sequence data (2014) (48)
- MUTATIONS IN THE GABRB1 GENE PROMOTE ALCOHOL CONSUMPTION THROUGH INCREASED TONIC INHIBITION (2013) (47)
- Schizophrenia susceptibility and chromosome 6p24–22 (1995) (47)
- Candidate genes and favoured loci: strategies for molecular genetic research into schizophrenia, manic depression, autism, alcoholism and Alzheimer's disease. (1986) (47)
- Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample (2011) (47)
- Genetic association of the tachykinin receptor 1 TACR1 gene in bipolar disorder, attention deficit hyperactivity disorder, and the alcohol dependence syndrome (2014) (44)
- Investigations into the genetics of alcohol dependence and into its effects on brain function. (1981) (44)
- Genome‐wide association analysis of age at onset and psychotic symptoms in bipolar disorder (2011) (43)
- Genetic linkage analysis supports the presence of two susceptibility loci for alcoholism and heavy drinking on chromosome 1p22.1-11.2 and 1q21.3-24.2 (2005) (43)
- Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (43)
- Molecular genetics of alcohol-related brain damage. (2009) (43)
- Linkage disequilibrium and demographic history of the isolated population of the Faroe Islands (2002) (42)
- Quantitative and molecular genetics of ADHD. (2012) (42)
- Linkage disequilibrium between two highly polymorphic microsatellites. (1991) (42)
- A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12 (1998) (41)
- DNA restriction fragment analysis of the proopiomelanocortin gene in schizophrenia and bipolar disorders. (1985) (40)
- The Relationship between Alcoholism and Neurosis: (1986) (39)
- Genetic linkage analysis of the X chromosome in autism, with emphasis on the fragile X region (2005) (37)
- No evidence for excess runs of homozygosity in bipolar disorder (2009) (37)
- Fine Mapping by Genetic Association Implicates the Chromosome 1q23.3 Gene UHMK1, Encoding a Serine/Threonine Protein Kinase, as a Novel Schizophrenia Susceptibility Gene (2007) (37)
- A genetic association study of chromosome 11q22-24 in two different samples implicates the FXYD6 gene, encoding phosphohippolin, in susceptibility to schizophrenia. (2007) (36)
- An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis (2014) (36)
- Genetic association study of GABRA2 single nucleotide polymorphisms and electroencephalography in alcohol dependence (2011) (34)
- Failure to find linkage and increased homozygosity for the dopamine D3 receptor gene in Tourette's syndrome (1993) (34)
- A gene expression and systems pathway analysis of the effects of clozapine compared to haloperidol in the mouse brain implicates susceptibility genes for schizophrenia (2012) (34)
- Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G‐protein signaling 4 protein (RGS4) (2006) (34)
- Failure to Confirm Allelic Association Between Markers at the CAPON Gene Locus and Schizophrenia in a British Sample (2006) (33)
- Allelic Association, DNA Resequencing and Copy Number Variation at the Metabotropic Glutamate Receptor GRM7 Gene Locus in Bipolar Disorder (2014) (32)
- The importance of alcohol misuse, malnutrition and genetic susceptibility on brain growth and plasticity (2007) (32)
- Genome‐wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness (2016) (32)
- Direct genomic PCR sequencing of the high affinity thiamine transporter (SLC19A2) gene identifies three genetic variants in Wernicke Korsakoff syndrome (WKS) (2005) (32)
- No evidence of expansion of CAG or GAA repeats in schizophrenia families and monozygotic twins (1998) (31)
- Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis (2019) (31)
- Unsound Methodology in Investigating a Pseudoautosomal Locus in Schizophrenia (1990) (31)
- A polygenic resilience score moderates the genetic risk for schizophrenia (2019) (31)
- Three-dimensional textural analysis of brain images reveals distributed grey-matter abnormalities in schizophrenia (2010) (30)
- Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1) (2001) (30)
- Genetic variants in or near ADH1B and ADH1C affect susceptibility to alcohol dependence in a British and Irish population (2015) (28)
- Genetic association, mutation screening, and functional analysis of a Kozak sequence variant in the metabotropic glutamate receptor 3 gene in bipolar disorder. (2013) (28)
- Two microsatellite polymorphisms at the D5S39 locus. (1991) (27)
- Genetic association and sequencing of the insulin‐like growth factor 1 gene in bipolar affective disorder (2011) (26)
- Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
- Application of molecular biology to mental illness. Analysis of genomic DNA and brain mRNA. (1985) (25)
- The Maudsley family study I: Structural brain changes on magnetic resonance imaging in familial schizophrenia (1997) (24)
- Point mutation analysis of the FMR-1 gene in autism. (1996) (24)
- Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia (2007) (23)
- Neuroreceptor subunit genes and the genetic susceptibility to gilles de la tourette syndrome (1997) (23)
- Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2018) (22)
- INCREASED CEREBRAL VENTRICULAR VOLUME IN MONOZYGOTIC TWINS DISCORDANT FOR ALCOHOLISM (1984) (22)
- A nonconservative amino acid change in the UPF3B gene in a patient with schizophrenia. (2012) (20)
- Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3 (2008) (20)
- Optimization of liposome mediated transfection of a neuronal cell line (1997) (20)
- Preliminary findings from a twin study of alcohol use. (1981) (20)
- European collaborative study of early‐onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset (2010) (19)
- Linkage analysis of manic depression (bipolar affective disorder) in Icelandic and British kindreds using markers on the short arm of chromosome 18. (1997) (18)
- Sequencing of the ANKYRIN 3 gene (ANK3) encoding ankyrin G in bipolar disorder reveals a non‐conservative amino acid change in a short isoform of ankyrin G (2012) (18)
- No evidence that extended tracts of homozygosity are associated with Alzheimer's disease (2011) (18)
- Psychological deficit from excessive alcohol consumption: evidence from a co-twin control study. (1991) (18)
- Current genetic and biological approaches to alcoholism. (1983) (18)
- Identification of the Slynar gene (AY070435) and related brain expressed sequences as a candidate gene for susceptibility to affective disorders through allelic and haplotypic association with bipolar disorder on chromosome 12q24. (2006) (17)
- Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder. (2015) (17)
- Investigation by Linkage Analysis of the XY Pseudoautosomal Region in the Genetic Susceptibility to Schizophrenia (1995) (17)
- Recent and future molecular genetic research into schizophrenia. (1989) (16)
- Refined linkage map of chromosome 5 in the region of the spinal muscular atrophy gene. (1993) (16)
- Mosaic copy number variation in schizophrenia (2013) (15)
- The genetic predisposition to alcohol dependence (1999) (15)
- Possible linkage of Tourette syndrome to markers on short arm of chromosome 3 (C3p21-14) (1990) (15)
- A novel polymorphism in exon 11 of the WKL1 gene, shows no association with schizophrenia (2002) (14)
- Frequency of the A1/A2 alleles of the D2 dopamine receptor (DRD2) gene in a British, Caucasian control group screened to exclude alcoholism and heavy drinking (1997) (13)
- Lack of evidence for close linkage of the glutamate GluR6 receptor gene with schizophrenia. (1996) (13)
- Tests of linkage and allelic association between markers in the 1p36 PRKCZ (Protein Kinase C Zeta) gene region and bipolar affective disorder (2012) (13)
- Increased brain radiodensity in alcoholism. A co-twin control study. (1986) (12)
- Platelet γ-aminobutyric acid-aminotransferase and monoamine oxidase in schizophrenia (1980) (12)
- Test of Xq26.3–28 linkage in bipolar and unipolar affective disorder in families selected for absence of male to male transmission (1997) (12)
- Exclusion of linkage of schizophrenia of the gene for the glutamate GluR5 receptor (1997) (11)
- Chromosome 21 workshop. (1998) (11)
- A cosmid clone for the 5HT1A receptor (HTR1A) reveals a TaqI RFLP that shows tight linkage to dna loci D5S6, D5S39, and D5S76. (1991) (11)
- Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (vol 41, pg 1088, 2009) (2013) (10)
- The effect of clozapine on mRNA expression for genes encoding G protein-coupled receptors and the protein components of clathrin-mediated endocytosis (2013) (10)
- Microsatellite polymorphisms for chromosome 5 bands q11.2-q13.3. (1993) (9)
- Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome (1998) (9)
- Genetic epidemiology in medicine--recent twin research. (1984) (9)
- Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms (2017) (9)
- A microsatellite polymorphism at the D3S11 locus. (1991) (8)
- Replication of genetic association studies between markers at the Epsin 4 gene locus and schizophrenia in two Han Chinese samples (2007) (8)
- GENETIC ASPECTS OF AFFECTIVE DISORDERS (1991) (7)
- Henrik Lykke Ewald (1958–2004) (2005) (7)
- Peer review policy (1992) (7)
- Genetic linkage and psychiatric disease (1990) (7)
- Lack of allelic association between markers at the DRD2 and ANKK1 gene loci with the alcohol-dependence syndrome and criminal activity. (2011) (6)
- Alcoholism: polygenic influence on a multifactorial disorder. (1982) (6)
- Exclusion of linkage between schizophrenia and the gene encoding a neutral amino acid glutamate/aspartate transporter, SLC1A5. (1996) (6)
- Act now against new NHS competition regulations (2013) (6)
- A linkage study of affective disorder with DNA markers for the ABO-AK1-ORM linkage group near the dopamine beta hydroxylase gene (1994) (5)
- Erratum to “Genome‐wide association analysis of age at onset and psychotic symptoms in bipolar disorder”, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics”, April 1; 156(3):370–378 (2011) (5)
- Analysis of Polymorphic Microsatellite DNA Sequences by PCR Amplification of Paraffin‐embedded Tissue: A Method of Genotyping Deceased Members of Pedigrees in Genetic Linkage Studies (1991) (5)
- Genomic imprinting in the Icelandic/ British schizophrenia study: Preliminary results (1993) (5)
- A linkage study with the D5 dopamine receptor in Icelandic pedigrees with multiple cases of manic depression (1993) (5)
- Testing the Retrovirus Hypothesis of Manic Depression and Schizophrenia with Molecular Genetic Techniques (1988) (4)
- Mortality and psychosis in twins. (1981) (4)
- Chromosome markers in Tourette's syndrome (1991) (4)
- Evidence for genetic susceptibility to the alcohol dependence syndrome from the thiamine transporter 2 gene solute carrier SLC19A3 (2014) (3)
- Mild learning difficulties and offending behaviour – is there a link with monoamine oxidase A deficiency? (2001) (3)
- Genetic influence, brain morphology, and cognitive deficits in alcoholic twins. (1987) (3)
- Lindage analysis in a large pedigree multiply affected with Gilles de la Tourette syndrome (1991) (3)
- Exon 11 of the chromosome 22 gene WKL1, previously shown to exhibit a base pair mutation in rare cases of schizophrenia, was found to contain an insertion/deletion polymorphism, affecting the receptor channel amino acid sequence. (2001) (2)
- Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
- Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease (2011) (2)
- Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (2)
- Genetic variant analysis of the putative regulatory regions of the LRRC7 gene in bipolar disorder. (2016) (2)
- Linkage analysis in a large pedigree multiply affected with Gilles de la Tourette syndrome (1991) (2)
- The role of genetic factors in the etiology of the affective disorders (1990) (2)
- Exclusion of linkage between schizophrenia and the putative chromosome 3p24-p26 susceptibility locus (1996) (2)
- Platelet gamma-aminobutyric acid-aminotransferase and monoamine oxidase in schizophrenia. (1980) (2)
- Ascertainment of families for a linkage study of alcoholism (2000) (2)
- GENETICS OF SCHIZOPHRENIA (1989) (2)
- Evidence of allelic association of bipolar disorder with two genes P2RX7 and AY070435 6 MB apart on 12q24 (2005) (1)
- Pseudoautosomal linkage in schizophrenia (1994) (1)
- A new journal for an expanding field (1990) (1)
- Genetics of schizophrenia. (2008) (1)
- IDENTIFICATION AND CHARACTERIZATION OF GENES SPANNING TRANSLOCATION BREAKPOINTS ON CHROMOSOME 7q31 IN TWO PATIENTS WITH AUTISTIC DISORDER (2000) (1)
- Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2019) (1)
- Molecular genetics and heterogeneity in manic depression (2008) (1)
- multiply affected with schizophrenia--the Maudsley Family Study 5. Brain changes in schizophrenia. Volumetric MRI study of families (2013) (1)
- Genatlas: A Catalogue of Mapped Genes and Other Markers (1991) (1)
- Sex of Parent Transmission Effect in Tourette's Syndrome: Age at Onset in Maternally Transmitted Cases Suggests a Genomic Imprinting Effect (1996) (1)
- 7 – Genetic linkage studies of schizophrenia (1991) (1)
- Principles of Psychiatric Genetics: The genetics of schizophrenia (2012) (1)
- MOLECULAR GENETIC INVESTIGATION INTO SCHIZOPHRENA AND BIPOLAR DISORDER: DNA POLYMORPHISMS OF THE GENE CODING for ACTH, ß ENDORPHIN, CLIP, α MSH AND ß LPH (1984) (1)
- Recent advances in the genetics of psychiatric disorder. (1990) (1)
- Erratum: Schizophrenia susceptibility and chromosome 6p24-22 (1996) (1)
- Loss of cerebral asymmetry in familial schizophrenia — a volumetric study using unbiased stereology (1997) (1)
- Collaborative Genome-Wide Analysis Supports a Role for ANK3 and CACNA1C in Bipolar Disorder (2009) (1)
- Psychological Aspects of Genetic Counselling. Edited by Alan E. H. Emery and Ian M. Pullen. Orlando: Academic Press. 1984. Pp. 236. $14.00/£9.00(pb), $32.00/£20.00 (hb). (1987) (1)
- Neuropsychological abnormalities in the relatives of familial and nonfamilial schizophrenics (1995) (1)
- An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation (2016) (1)
- Identification of a model of alcohol preference and its similarity to human alcoholism (2008) (0)
- Failure to confirm association between schizophrenia and markers on chromosome 1q23.3 at the RGS4 and CAPON genes (2005) (0)
- CONNECTIVITY GENES IN COMORBID ALCOHOLISM AND BIPOLAR DISORDER (2010) (0)
- Failure to confirm allelic association between COMT and bipolar disorder in a large UK sample (2006) (0)
- A search for the risk allele for bipolar affective disorder on chromosome 12q24.2. (2000) (0)
- Loss of Developmental Torque in Familial Schizophrenia — a Volumetric Magnetic Resonance Imaging Study Using Unbiased Stereology (1996) (0)
- Diagnostic issues in the study of schizophrenia genetics (1990) (0)
- Association study between patients with bipolar disorder and markers from the candidate region on chromosome 12q24.2-12q24.3. (1999) (0)
- A genetic association study implicates the chromosome 11q23.3 gene FXYD6 encoding phopshohippolin in susceptibility to schizophrenia in University College London and Aberdeen case control samples (2007) (0)
- GENOMIC CLONING, LOCALIZATION AND IDENTIFICATION OF A HIGHLY POLYMOROHIC MICROSATELLITE SEQUENCE FOR THE D5-DOPAMINE NEURORECEOTOR GENE LOCUS (DRD5) ON CHROMOSOME-4P WHICH SHOWS NO LINKAGE TO SCHIZOPHRENIA, MANIC-DEPRESSION AND TOURETTE SYNDROME (1993) (0)
- Fine mapping of a new bipolar and unipolar affective disorder locus on chromosome 1p36 (2006) (0)
- A TaqI polymorphism detected by a genomic clone at the locus D5S39 (5q11-13). (1991) (0)
- Gene brain structure relationships: arbitrary assumptions of heterogeneity generate unfalsifiable claims. (2007) (0)
- Detection and Characterisation of the Bipolar Susceptibility Gene Slynar in the Mouse (2006) (0)
- Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (0)
- Age of onset in familial schizophrenia: Icelandic/British study (1993) (0)
- Institution: UCL (2013) (0)
- Detection of potential aetiological base pair changes causing genetic susceptibility to schizophrenia in the pericentriolar material 1 (PCM1) gene on chromosome 8p22 supports evidence from allelic association (2005) (0)
- In Memoriam: Henrik Lykke Ewald (25.11.1958???20.01.2004) (2005) (0)
- Allelic and haplotypic association with bipolar disorder implicates a 300 kilobase region on chromosome 12q24.3 containing novel brain expressed gene sequences (2005) (0)
- UK 10 K Consortium (2019) (0)
- Relatives at Risk for Mental Disorders. Edited by David L. Dunner, Elliot S. Gershon and James E. Barrett. New York: Raven. 1988. 324 pp. $99.00. (1988) (0)
- PSYCHOMETRIC TESTING AND CT SCANS OF LONG-TERM OPIATE ADDICTS (1991) (0)
- Gene therapy for neuropsychiatric disorders: liposome-mediated gene transfer in organotypic explant cultures from the CNS (1996) (0)
- 22 . 1-11 . 2 and 1 q 21 . 3-24 . 2 (2015) (0)
- PSEUDOAUTOSOMAL LINKAGE IN SCHIZOPHENIA. AUTHOR'S REPLY (1994) (0)
- Psychiatric Genetics 2nd World Congress Abstracts Editorial Introduction (1991) (0)
- UPDATE ON THE ANALYSES OF THE LARGEST BIPOLAR CASE-CONTROL EXOME SEQUENCING DATASET TO DATE (2019) (0)
- Detection and characterisation of the bipolar suspectibility gene Slynar in human cell lines (2008) (0)
- Universitet Low-frequency variation in TP 53 has large effects on head circumference and intracranial (2019) (0)
- The search for an endophenotype correlated with a subtype of schizophrenia: Magnetic resonance imaging in two large British Pedigrees (1992) (0)
- Support for BRD1 as a suspectibility gene for both schizophrenia and bipolar affective disorder (2007) (0)
- Erratum A microsatellite polymorphism at D3S11 locus (1992) (0)
- The Instruments of Psychiatric Research. Edited by Chris Thompson. Chichester: John Wiley. 1989. 345 pp. £35.00. (1990) (0)
- Kenneth John Gurling (2003) (0)
- Estimation of haplotypes at DRD2 may have produced misleading results. (2006) (0)
- WHAT CAN NK1R (/) MICE TELL US ABOUT ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD)? (2010) (0)
- VKučinskas-2001-2016 (2016) (0)
- Non-viral gene therapy of the CNS: optimization of DC-CHOL (1996) (0)
- Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
- The genetics of mood disorders (1992) (0)
- DNA Probes, 2nd edition (1995) (0)
- Sib-pair study of early onset bipolar affective disorder: Preliminary results of a genome scan (2004) (0)
- Molecular genetic research in schizophrenia (1991) (0)
- Psychiatric genetics and studies of relatives of psychotic patients (2010) (0)
- 65 IDENTIFYING SUSCEPTIBILITY LOCI FOR TOURETTE'S SYNDROME IN A DENSELY AFFECTED PEDIGREE (2019) (0)
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